Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11142387 9 70383416 downstream gene variant A/C snv 0.49 7
rs9983925
ADARB1
21 45216929 intron variant C/T snv 0.46 4
rs4675690 2 207643083 intergenic variant C/T snv 0.48 3
rs1009080 1 29958713 intergenic variant G/A snv 0.54 2
rs10496702
NCKAP5
2 133247997 intron variant G/A snv 0.18 2
rs10949808 7 156255955 intergenic variant T/G snv 0.45 2
rs11164835
DIPK1A
1 92913536 intron variant G/A snv 0.35 2
rs11740562
ADAM19
5 157515277 intron variant A/G snv 7.1E-02 2
rs11789407
LOC105376249
9 118597268 intergenic variant C/A snv 0.44 2
rs12282742
SAA2-SAA4 ; SAA2
11 18244252 intron variant C/G;T snv 2
rs12527359 6 89018502 intergenic variant T/A snv 0.23 2
rs12745968
DIPK1A
1 92936280 intron variant A/G snv 0.36 2
rs17069122 6 108002555 downstream gene variant G/A snv 1.9E-02 2
rs17075286 3 43189231 intergenic variant C/G snv 5.9E-02 2
rs1799920
HTR1A
5 63961656 missense variant C/G;T snv 3.2E-04 2
rs1799921
HTR1A
5 63961638 missense variant T/C snv 9.4E-03 9.3E-03 2
rs1806864 9 87416754 regulatory region variant G/C snv 7.4E-02 2
rs1992044
LOC105375856 ; LINC01602
8 57928349 intron variant G/A;T snv 2
rs1992045
LOC105375856 ; LINC01602
8 57928365 intron variant C/T snv 0.14 2
rs2018368 11 10718819 intergenic variant C/G snv 0.59 2
rs2044117
NALCN ; NALCN-AS1
13 101055958 intron variant G/A snv 0.19 2
rs2049161
DLGAP1
18 4127583 intron variant A/C;T snv 0.22 2
rs2155907 11 98223945 intergenic variant C/T snv 0.38 2
rs2509843 11 98254676 intergenic variant A/C;G;T snv 2
rs2841307 6 100308811 intergenic variant C/T snv 0.20 2